ZOLL AED Plus 2010 Guidelines Upgrade, Ten Kit (CD and Overlay Label Sets)

AED-Plus-2010-Guidelines-Upgrade-Single Kit-CD-and-One-Overlay-Label-Set

Additional Images

  • AED-Plus-2010-Guidelines-Upgrade-Single Kit-CD-and-One-Overlay-Label-Set

ZOLL AED Plus 2010 Guidelines Upgrade, Ten Kit (CD and Overlay Label Sets)

Product Code 7771-000010-01

0 reviews

In Stock

What's Included?

  • ZOLL Administrative software
  • One overlay label set
  • Overlay label placement instructions
  • AED Plus upgrade instructions
  • Software update acknowledgement card

The AED Plus 2010 Guidelines Upgrade, Ten Kit from ZOLL will enable you to upgrade your ZOLL AED Plus to the 2010 Guidelines from the American Heart Association. In this specific variation you are provided with 10 sets of the kit.

Ensuring you’re delivering the most up-to-date treatment to the victim of sudden cardiac arrest will provide them with the highest chance of survival. This treatment can only be provided if your AED is up-to-date and this kit can help ensure your AED contains the 2010 American Heart Association treatment guidelines.

The overlay labels are to be used to modify the current face of the AED and update the diagrams so the treatment being delivered matches the treatment steps on the AED.

ZOLL’s administration software (ZAS), is compatible with the following systems:

  • Windows XP
  • Windows 2000
  • Windows Vista
  • Windows 7

Please note: this software is not compatible with Mac OS.

About the Manufacturer

ZOLL Medical all started with the Chief of the Cardiac Clinic at Beth Israel Hospital, Paul M. Zoll back in 1952.

Over the decades they have become famous for their strikingly unmissable green devices which stand out in almost any environment and cater for all training levels of responders, from medical professionals and first-time rescuers.

More Information

If you would like to learn more about the AED Plus 2010 Guidelines Upgrade, Ten Kit (CD and Overlay Label Sets), the team here at defibshop are here to help.

Call 888 820 0760 to speak to one of our experts and they’ll be happy to help in any way they can.

 Want to know why you should choose us? 

  • Experienced and knowledgeable staff on-hand to offer impartial advice on all things AEDs
  • We have a nationwide training network to deliver training in the use of a defib and CPR
  • Not only providing free battery and pad reminders, we also will replace your electrode pads for free if you use your defib in the first two years after purchase
  • Over 14 years worth of experience as an AED specialist 
  • 5 / 5 Review Score
  • Over 97% of our customers would buy from us again

 

What is an IP rating?

An IP (Ingress Protection) rating classifies the degrees of protection of an electrical item against water and dust. Beginning with IP and followed by two numbers, the first digit is indicative of the item’s resistance to dust and the second is of its resistance to water. Protection against dust is measured from */ 0 up to 6, whereas protection against water is measured from */ 0 up to 8. The protection against these elements increases as the number does, with * / 0 telling us that the item has NO protection against either dust or water.

Why is this important?

The IP rating of a defib will tell you (and us!) whether it is suitable for the environment where it’s most likely to be used; for example, if there is a good chance your defib may be used in an outdoor environment, you will need a unit with a higher IP rating to ensure it can be used regardless the weather or terrain. If you are looking for a defibrillator more suitable for an indoors environment, you can afford to choose one with a lower IP rating, based on the other features that may be more suitable.

When a particular product is “approved” by the FDA, this marks the pass in the premarket approval (or PMA) application of a particular product which has been submitted to the FDA.

To receive approval of a device through a PMA application, the applicant in question must provide reasonable assurance of the device’s safety and effectiveness which is then challenged by the FDA before being approved.

Whilst all AEDs can be used to increase chances of survival and even save a life in the event of a cardiac arrest, FDA approved devices provide that extra piece of mind that the specific unit being used has undergone vigorous and substantial testing to ensure that that particular piece of equipment operates just as it should and provides the most effective care possible.

Many manufacturers perform their own tests on products, but not all defibrillators will undergo the same premarket approval as FDA approved devices and there is no guarantee or stamp of certification if testing has taken place with non-FDA approved products.